Sr. QPPV Office (QPO) Specialist

Join our global Pharmacovigilance team as a Sr. QPPV Office (QPO) Specialist.

Sr. QPPV Office (QPO) Specialist is responsible for the development of pharmacovigilance systems, and the oversight of end-to-end pharmacovigilance activities and projects’ compliance with Quality Management System as well as the reporting and exchanging of safety and pharmacovigilance information for medicinal products.

Position is in any EU country.

Responsibilities :

• Manage full Pharmacovigilance systems and projects (or part of them)
• Promote, maintain, improve compliance with Pharmacovigilance (PV) tasks and responsibilities
• May act as Regional QPPV or deputy
• Influence the performance of the quality system and PV activities
• Develop, update, and review standard operating procedures for global pharmacovigilance processes, and implement changes to fulfill requirements
• Supervise, prepare and submit PSURs, Risk Management Plans and risk minimization activities
• Be the primary point of contact for PV-related matter Ensure oversight of the contractual partner safety data exchange agreements
• Ensure the survey and monitoring of European (including UK) level pharmacovigilance regulations
• Provide Pharmacovigilance trainings
• Ensure continuous safety profile monitoring, detection of new signals and evaluation
• Communication with Competent Authorities
• Participate in related inspection and / or audits

Requirements

Benefits